Pregabalin produces analgesia in males but not females in an animal model of chronic widespread muscle pain.

IF 3.4 Q2 NEUROSCIENCES
Pain Reports Pub Date : 2024-11-20 eCollection Date: 2024-12-01 DOI:10.1097/PR9.0000000000001207
Ashley N Plumb, Kazuhiro Hayashi, Adam Janowski, Angela Smith, Lynn Rasmussen, Kathleen A Sluka, Joseph B Lesnak
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引用次数: 0

Abstract

Introduction: Pregabalin, which acts on the α2δ-1 subunit of voltage-gated calcium channels, relieves ≥50% of pain in a third of individuals with fibromyalgia. Thus far, preclinical studies of pregabalin have predominantly used male animals.

Objectives: The purpose of our study was to investigate potential sex differences in the analgesic efficacy of pregabalin that may contribute to disparities in human outcomes.

Methods: We used a mouse model of chronic widespread muscle pain (CWP) to test the effects of pregabalin on muscle hyperalgesia, nonreflexive pain, and motor behaviors. The CWP pain model combines 2 pH 4.0 saline injections, spaced 5 days apart, into the gastrocnemius muscle and produces bilateral muscle hyperalgesia. Furthermore, we explored sex differences in the mRNA and protein expression of the α2δ-1 subunit of voltage-gated calcium channels in the dorsal horn of the spinal cord and dorsal root ganglia after development of CWP.

Results: Pregabalin fully attenuated muscle hyperalgesia bilaterally in male but not female mice with equal motor deficits produced in both sexes. In addition, using the conditioned place preference test, mice of both sexes with CWP spent significantly more time in the pregabalin-paired chamber compared with baseline, but not significantly greater than pain-free controls. Chronic widespread muscle pain produced no changes in α2δ-1 subunit mRNA or protein expression in the dorsal horn of the spinal cord or dorsal root ganglia in either sex.

Conclusion: Overall, these findings indicate pregabalin may be more effective in treating CWP in males, but the factors leading to these differences are not fully understood.

在慢性广泛性肌肉疼痛动物模型中,普瑞巴林对雄性动物产生镇痛作用,而对雌性动物则没有。
简介普瑞巴林作用于电压门控钙通道的α2δ-1亚基,可缓解三分之一纤维肌痛患者≥50%的疼痛。迄今为止,普瑞巴林的临床前研究主要使用雄性动物:我们研究的目的是调查普瑞巴林镇痛效果中潜在的性别差异,这种差异可能会导致人类结果的差异:我们使用慢性广泛性肌肉疼痛(CWP)小鼠模型来测试普瑞巴林对肌肉超痛觉、非反射性疼痛和运动行为的影响。CWP 疼痛模型是在腓肠肌注射 2 次 pH 值为 4.0 的生理盐水,间隔 5 天,产生双侧肌肉痛觉减退。此外,我们还探讨了CWP发生后脊髓背角和背根神经节中电压门控钙通道α2δ-1亚基的mRNA和蛋白表达的性别差异:结果:普瑞巴林能完全缓解雄性小鼠双侧肌肉的痛觉减退,但不能完全缓解雌性小鼠双侧肌肉的痛觉减退,且雌雄小鼠产生的运动障碍程度相同。此外,通过条件性位置偏好试验,患有 CWP 的雌雄小鼠在普瑞巴林配对的小室中停留的时间明显多于基线时间,但不明显多于无痛对照组。慢性广泛性肌肉疼痛对雌雄小鼠脊髓背角或背根神经节中的α2δ-1亚基mRNA或蛋白质表达均无影响:总之,这些研究结果表明普瑞巴林对治疗男性 CWP 可能更有效,但导致这些差异的因素尚不完全清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pain Reports
Pain Reports Medicine-Anesthesiology and Pain Medicine
CiteScore
7.50
自引率
2.10%
发文量
93
审稿时长
8 weeks
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